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Cellosaurus CRICKi009-A (CVCL_C5T1)

[Text version]
Cell line name CRICKi009-A
Synonyms iFCI012 Clone 4; iBK983
Accession CVCL_C5T1
Resource Identification Initiative To cite this cell line use: CRICKi009-A (RRID:CVCL_C5T1)
Comments From: The Francis Crick Institute Limited; London; United Kingdom.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:12687; VHL; Simple; p.Val137Cysfs*22 (c.409delG); Zygosity=Heterozygous (PubMed=39549334).
Disease Von Hippel-Lindau syndrome (NCIt: C3105)
Von Hippel-Lindau disease (ORDO: Orphanet_892)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 22Y
Category Induced pluripotent stem cell
Publications

PubMed=39549334; DOI=10.1016/j.scr.2024.103611
Devito L.G., Lim E.S.-Y., O'Toole S.M., Shepherd S.T.C., Deng D.-Q., Feng H.-G., Barber T., Drake W.M., Turajlic S., Healy L.E.
Generation of two iPSC lines (CRICKi009-A; CRICKi010-A) from patients with type 1 von Hippel-Lindau (VHL) and histopathologically confirmed renal cell carcinoma (RCC).
Stem Cell Res. 81:103611-103611(2024)

Cross-references
Cell line databases/resources hPSCreg; CRICKi009-A
Biological sample resources BioSamples; SAMEA112239881
Encyclopedic resources Wikidata; Q116048792
Entry history
Entry creation15-Dec-2022
Last entry update10-Apr-2025
Version number5